U.S. flag

An official website of the United States government

nsv6990004

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:30,125

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 327 SVs from 45 studies. See in: genome view    
    Submitted genomic75,564,097-75,594,221Question Mark
    Overlapping variant regions from other studies: 327 SVs from 45 studies. See in: genome view    
    Remapped(Score: Perfect):73,560,178-73,590,302Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6990004Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1775,564,09775,594,221
    nsv6990004RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1773,560,17873,590,302

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18631300duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18631300Submitted genomicNC_000017.11:g.755
    64097_75594221dup
    GRCh38 (hg38)NC_000017.11Chr1775,564,09775,594,221
    nssv18631300RemappedPerfectNC_000017.10:g.735
    60178_73590302dup
    GRCh37.p13First PassNC_000017.10Chr1773,560,17873,590,302

    No validation data were submitted for this variant

    No clinical assertion data were submitted for this variant

    Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

    Genotype Information

    Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
    nssv186313004e-061275764
    Support Center